Globe-Trotter GT5400

FDA 510(k) K141565 · Draeger Medical Systems, Inc.

Substantially Equivalent

510(k) numberK141565

Submission

Device name
Globe-Trotter GT5400
Applicant
Draeger Medical Systems, Inc.
Telford, PA, US
Received
June 12, 2014
Decision date
September 10, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FPL – Incubator, Neonatal Transport
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5410
Specialty
General Hospital

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Questions and answers

When was Globe-Trotter GT5400 cleared by the FDA?

Globe-Trotter GT5400 (K141565) received a 510(k) decision of Substantially Equivalent on September 10, 2014, 90 days after the submission was received.

What is the product code of K141565?

The FDA product code is FPL – Incubator, Neonatal Transport, a Class II (moderate risk) device regulated under 21 CFR 880.5410.